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                             23 gevonden resultaten
nr titel auteur tijdschrift jaar jaarg. afl. pagina('s) type
1 A Family-Centered Model for Sharing Genetic Risk Daly, Mary B.
2015
43 3 p. 545-551
artikel
2 Calendar of Events 2015
43 3 p. 666
artikel
3 Canadian Research Ethics Board Leadership Attitudes to the Return of Genetic Research Results to Individuals and Their Families Fernandez, Conrad V.
2015
43 3 p. 514-522
artikel
4 Certificates of Confidentiality: Protecting Human Subject Research Data in Law and Practice Wolf, Leslie E.
2015
43 3 p. 594-609
artikel
5 Considerations for Returning Research Results to Culturally Diverse Participants and Families of Decedents Garrison, Nanibaa' A.
2015
43 3 p. 569-575
artikel
6 Considering Actionability at the Participant's Research Setting Level for Anticipatable Incidental Findings from Clinical Research Ortiz-Osorno, Alberto (Betto)
2015
43 3 p. 619-632
artikel
7 Disclosing Secondary Findings from Pediatric Sequencing to Families: Considering the “Benefit to Families” Wilfond, Benjamin S.
2015
43 3 p. 552-558
artikel
8 Ethical Integrity in Health Care Organizations: Currents in Contemporary Bioethics Mantel, Jessica
2015
43 3 p. 661-665
artikel
9 Funding the Costs of Disease Outbreaks Caused by Non-Vaccination Moser, Charlotte A.
2015
43 3 p. 633-647
artikel
10 How Agencies Market Egg Donation on the Internet: A Qualitative Study Keehn, Jason
2015
43 3 p. 610-618
artikel
11 How Much Control Do Children and Adolescents Have over Genomic Testing, Parental Access to Their Results, and Parental Communication of Those Results to Others? Clayton, Ellen Wright
2015
43 3 p. 538-544
artikel
12 International Policies on Sharing Genomic Research Results with Relatives: Approaches to Balancing Privacy with Access Branum, Rebecca
2015
43 3 p. 576-593
artikel
13 Mapping the Ethics of Translational Genomics: Situating Return of Results and Navigating the Research-Clinical Divide Wolf, Susan M.
2015
43 3 p. 486-501
artikel
14 Patients' Choices for Return of Exome Sequencing Results to Relatives in the Event of Their Death Amendola, Laura M.
2015
43 3 p. 476-485
artikel
15 Pediatric Cancer Genetics Research and an Evolving Preventive Ethics Approach for Return of Results after Death of the Subject Scollon, Sarah
2015
43 3 p. 529-537
artikel
16 Physician Dismissal of Families Who Refuse Vaccination: An Ethical Assessment Diekema, Douglas S.
2015
43 3 p. 654-660
artikel
17 Preferences regarding Return of Genomic Results to Relatives of Research Participants, Including after Participant Death: Empirical Results from a Cancer Biobank Breitkopf, Carmen Radecki
2015
43 3 p. 464-475
artikel
18 Returning a Research Participant's Genomic Results to Relatives: Analysis and Recommendations Wolf, Susan M.
2015
43 3 p. 440-463
artikel
19 Returning a Research Participant's Genomic Results to Relatives: Perspectives from Managers of Two Distinct Research Biobanks Petersen, Gloria M.
2015
43 3 p. 523-528
artikel
20 Return of Genetic Research Results to Participants and Families: IRB Perspectives and Roles Beskow, Laura M.
2015
43 3 p. 502-513
artikel
21 Return of Research Results: What about the Family? Wolf, Susan M.
2015
43 3 p. 437-439
artikel
22 Return of Results from Research Using Newborn Screening Dried Blood Samples Lewis, Michelle Huckaby
2015
43 3 p. 559-568
artikel
23 The Pediatrician's Dilemma: Refusing the Refusers of Infant Vaccines Block, Stan L.
2015
43 3 p. 648-653
artikel
                             23 gevonden resultaten
 
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